LDH info

Canonical Allele Identifier: CA130208
Gene: GNRHR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 16031
dbSNP Id: rs104893843

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754306A>T , CM000666.2:g.67754306A>T GRCh38
NC_000004.11:g.68620024A>T , CM000666.1:g.68620024A>T GRCh37
NC_000004.10:g.68302619A>T NCBI36
NG_009293.1:g.6781T>A

Transcript Alleles

HGVS Amino-acid change
NM_000406.2:c.30T>A VV NP_000397.1:p.Asn10Lys
NM_001012763.1:c.30T>A VV NP_001012781.1:p.Asn10Lys
NM_000406.3:c.30T>A VV NP_000397.1:p.Asn10Lys
NM_001012763.2:c.30T>A VV NP_001012781.1:p.Asn10Lys
ENST00000226413.4:c.30T>A ENSP00000226413.4:p.Asn10Lys
ENST00000420975.2:n.30T>A ENSP00000397561.2:p.Asn10Lys